Canonical Allele Identifier: CA360410370

Gene: ADGRV1

Linked Data

• COSMIC: COSM141939
• MyVariant Identifiers: chr5:g.90106721C>T (hg19) ; chr5:g.90810904C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90810904C>T , CM000667.2:g.90810904C>T	GRCh38
NC_000005.9:g.90106721C>T , CM000667.1:g.90106721C>T	GRCh37
NC_000005.8:g.90142477C>T	NCBI36
NG_007083.1:g.257105C>T
NG_007083.2:g.286561C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.15644C>T MANE Select	ENSP00000384582.2:p.Ser5215Phe
ENST00000425867.3:c.4598C>T	ENSP00000392618.3:p.Ser1533Phe
ENST00000638510.1:n.2911C>T
ENST00000639431.1:c.265+134695C>T	ENSP00000491057.1:n.265+134695C>T
ENST00000640407.1:c.2054C>T	ENSP00000491425.1:p.Ser685Phe
ENST00000405460.6:c.15644C>T	ENSP00000384582.2:p.Ser5215Phe
ENST00000425867.2:c.2627C>T	ENSP00000392618.2:p.Ser876Phe
NM_032119.3:c.15644C>T	NP_115495.3:p.Ser5215Phe
NR_003149.1:n.15657C>T
XM_011543675.1:c.15641C>T	XP_011541977.1:p.Ser5214Phe
XM_011543676.1:c.15563C>T	XP_011541978.1:p.Ser5188Phe
XM_011543677.1:c.12947C>T	XP_011541979.1:p.Ser4316Phe
NM_032119.4:c.15644C>T MANE Select	NP_115495.3:p.Ser5215Phe
XM_017009963.2:c.15665C>T	XP_016865452.1:p.Ser5222Phe
XM_017009964.2:c.15662C>T	XP_016865453.1:p.Ser5221Phe
XM_017009965.1:c.15662C>T	XP_016865454.1:p.Ser5221Phe
XM_017009966.2:c.15584C>T	XP_016865455.1:p.Ser5195Phe
XM_017009967.1:c.15569C>T	XP_016865456.1:p.Ser5190Phe
XM_017009968.2:c.15485C>T	XP_016865457.1:p.Ser5162Phe
XM_017009969.2:c.15665C>T	XP_016865458.1:p.Ser5222Phe
XM_017009972.1:c.8783C>T	XP_016865461.1:p.Ser2928Phe
XM_017009973.1:c.8762C>T	XP_016865462.1:p.Ser2921Phe
NR_003149.2:n.15660C>T